Literature DB >> 8220478

Differences in DNA-methylation are associated with a paramutation phenomenon in transgenic petunia.

P Meyer1, I Heidmann, I Niedenhof.   

Abstract

The transgenic petunia line 17-R contains one copy of the maize A1 gene which mediates brick-red pelargonidin pigmentation of the flower. A white derivative, 17-W, was isolated from homozygous progeny of this line in which no pelargonidin pigmentation was observed. In 17-W the 35S promoter driving the A1 gene was hypermethylated, in contrast to its hypomethylated state in 17-R. Progeny plants carrying both the 17-R and 17-W allele did not show the expected A1 phenotype. Predominantly white progeny and variable plants were observed which showed a continuous change in pattern and intensity of pelargonidin pigmentation. This reduction of A1 activity argues for a semidominant effect of the 17-W allele which inhibits the activity of its homologue, 17-R. This system shows striking similarities to some paramutation phenomena in plants which represent a heritable change in gene function of a paramutable allele directed by a paramutagenic homologue. The analysis of the methylation patterns of the A1 alleles suggests that interactions between differentially methylated alleles are responsible for the paramutation-like effect which is mediated by somatic pairing. The analogy of this system to other phenomena based on homology-dependent interlocus trans-inactivation supports the assumption that those may be based on a related mechanism which includes an interaction between ectopic homologues.

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Year:  1993        PMID: 8220478     DOI: 10.1046/j.1365-313x.1993.04010089.x

Source DB:  PubMed          Journal:  Plant J        ISSN: 0960-7412            Impact factor:   6.417


  66 in total

1.  The structure and paramutagenicity of the R-marbled haplotype of Zea mays.

Authors:  T Panavas; J Weir; E L Walker
Journal:  Genetics       Date:  1999-10       Impact factor: 4.562

2.  Expression and sequence requirements for nitrite reductase co-suppression.

Authors:  P Crété; H Vaucheret
Journal:  Plant Mol Biol       Date:  1999-09       Impact factor: 4.076

3.  The frequency of silencing in Arabidopsis thaliana varies highly between progeny of siblings and can be influenced by environmental factors.

Authors:  T J Meza; D Kamfjord; A M Håkelien; I Evans; L H Godager; A Mandal; K S Jakobsen; R B Aalen
Journal:  Transgenic Res       Date:  2001       Impact factor: 2.788

4.  Paramutation alters regulatory control of the maize pl locus.

Authors:  J B Hollick; G I Patterson; I M Asmundsson; V L Chandler
Journal:  Genetics       Date:  2000-04       Impact factor: 4.562

5.  The late developmental pattern of Mu transposon excision is conferred by a cauliflower mosaic virus 35S -driven MURA cDNA in transgenic maize.

Authors:  M N Raizada; V Walbot
Journal:  Plant Cell       Date:  2000-01       Impact factor: 11.277

6.  Transgene integration into the same chromosome location can produce alleles that express at a predictable level, or alleles that are differentially silenced.

Authors:  C D Day; E Lee; J Kobayashi; L D Holappa; H Albert; D W Ow
Journal:  Genes Dev       Date:  2000-11-15       Impact factor: 11.361

Review 7.  The rest is silence.

Authors:  E Bernstein; A M Denli; G J Hannon
Journal:  RNA       Date:  2001-11       Impact factor: 4.942

Review 8.  Systemic silencing signal(s).

Authors:  M Fagard; H Vaucheret
Journal:  Plant Mol Biol       Date:  2000-06       Impact factor: 4.076

Review 9.  Plants as bioreactors for protein production: avoiding the problem of transgene silencing.

Authors:  C De Wilde; H Van Houdt; S De Buck; G Angenon; G De Jaeger; A Depicker
Journal:  Plant Mol Biol       Date:  2000-06       Impact factor: 4.076

Review 10.  Role of inverted DNA repeats in transcriptional and post-transcriptional gene silencing.

Authors:  M W Muskens; A P Vissers; J N Mol; J M Kooter
Journal:  Plant Mol Biol       Date:  2000-06       Impact factor: 4.076

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